DocumentCode :
693358
Title :
Preparation of hyperactive etherifying agent of glycidyltriethylammonium chloride
Author :
Zongcheng Miao ; Fang Wang ; Deng Deng
Author_Institution :
Xijing Univ., Xi´an, China
Volume :
2
fYear :
2014
fDate :
19-21 Aug. 2014
Firstpage :
601
Lastpage :
603
Abstract :
[Purpose] In order to reducing the toxicity of general cationic surfactants, biodegradable ester cationic surfactants have been developed as novel kinds of environmental products in the world. [Method] Hyperactive etherifying agent of glycidyltriethyl ammonium chloride is very important intermediate product to synthesis biodegradable ester cationic surfactants. In this paper, a kind of hyperactive etherifying agent of glycidyltriethylammonium chloride was synthesized by traditional method with epichlorohydrin and trimethylamine as raw materials. [Results] During the synthesis, the best reaction conditions have been obtained, that the reaction temperature is 25 oC, the reaction time is 3 h, the reaction solvent is acetone, and the best mol ratio of epichlorohydrin to timethylamine is 3:1. [Conclusions] In addition, the chemical structure of the product has been confirmed by FT-IR, it is conformed with glycidyltriethylammonium chloride completely.
Keywords :
Fourier transform spectra; chemical reactions; chemical structure; crystal growth from solution; infrared spectra; organic compounds; FTIR; acetone; biodegradable ester cationic surfactants; chemical structure; epichlorohydrin; glycidyltriethyl ammonium chloride; hyperactive etherifying agent; reaction solvent; temperature 25 degC; time 3 h; trimethylamine; Chemicals; Equations; Fabrics; Liquids; Raw materials; Solvents; Vibrations; Cationic surfactant; Epoxy intermediate; Etherifying agent; FT-IR;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Materials for Renewable Energy and Environment (ICMREE), 2013 International Conference on
Conference_Location :
Chengdu
Print_ISBN :
978-1-4799-3335-8
Type :
conf
DOI :
10.1109/ICMREE.2013.6893745
Filename :
6893745
Link To Document :
بازگشت